CETP, cholesteryl ester transfer protein, 1071

N. diseases: 157; N. variants: 24
Source: BEFREE ×
Disease Type Disease Class Semantic Type N. genes d N. SNPs d Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
CUI: C0342890
Disease: Primary combined hyperlipidemia
Primary combined hyperlipidemia 		disease Disease or Syndrome 1 0.010 None 1.000 1 2009 2009
CUI: C3151466
Disease: HEPATIC LIPASE DEFICIENCY (disorder)
HEPATIC LIPASE DEFICIENCY (disorder) 		disease Nutritional and Metabolic Diseases Disease or Syndrome 5 2 0.010 None 1.000 1 2008 2008
CUI: C3875011
Disease: Familial hyperalphalipoproteinemia
Familial hyperalphalipoproteinemia 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 5 0.010 None 1.000 1 1993 1993
CUI: C0268601
Disease: HMG CoA lyase deficiency
HMG CoA lyase deficiency 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 6 0.010 None 1.000 1 2008 2008
CUI: C0856737
Disease: Single vessel disease
Single vessel disease 		disease Cardiovascular Diseases Disease or Syndrome 6 0.010 None 1.000 1 2005 2005
CUI: C0948480
Disease: Coronary Restenosis
Coronary Restenosis 		disease Cardiovascular Diseases Disease or Syndrome 6 1 0.010 None < 0.001 1 2010 2010
CUI: C2047520
Disease: Mixed hyperlipidemia (disorder)
Mixed hyperlipidemia (disorder) 		disease Nutritional and Metabolic Diseases Disease or Syndrome 6 3 0.010 None 1.000 1 2019 2019
CUI: C0342879
Disease: Primary hypercholesterolemia
Primary hypercholesterolemia 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 7 2 0.030 None 1.000 3 2002 2017
CUI: C3149462
Disease: HYPERALPHALIPOPROTEINEMIA 1
HYPERALPHALIPOPROTEINEMIA 1 		disease Disease or Syndrome 9 1 0.800 limited 0.933 27 1 1990 2018
CUI: C0271738
Disease: Hypocortisolism secondary to another disorder
Hypocortisolism secondary to another disorder 		disease Endocrine System Diseases Disease or Syndrome 13 0.010 None 1.000 1 2017 2017
CUI: C0856738
Disease: Triple vessel disease
Triple vessel disease 		disease Cardiovascular Diseases Disease or Syndrome 13 3 0.010 None 1.000 1 2005 2005
CUI: C0948387
Disease: Secondary Adrenal Insufficiency
Secondary Adrenal Insufficiency 		disease Endocrine System Diseases Disease or Syndrome 14 0.010 None 1.000 1 2017 2017
CUI: C1299433
Disease: Left main coronary artery disease
Left main coronary artery disease 		disease Cardiovascular Diseases Disease or Syndrome 17 4 0.010 None < 0.001 1 1 2011 2011
CUI: C0263420
Disease: Hyperkeratosis lenticularis perstans
Hyperkeratosis lenticularis perstans 		disease Skin and Connective Tissue Diseases Disease or Syndrome 18 11 0.020 None 1.000 2 1994 2001
CUI: C1704429
Disease: Hypoalphalipoproteinemia, Familial
Hypoalphalipoproteinemia, Familial 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 18 0.010 None 1.000 1 2014 2014
CUI: C0342388
Disease: Adrenocorticotropic hormone (ACTH) deficiency (disorder)
Adrenocorticotropic hormone (ACTH) deficiency (disorder) 		disease Endocrine System Diseases Disease or Syndrome 19 1 0.010 None 1.000 1 2008 2008
CUI: C0473527
Disease: Hypoalphalipoproteinemias
Hypoalphalipoproteinemias 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 20 7 0.020 None 0.500 2 1995 2019
CUI: C0302314
Disease: Xanthoma
Xanthoma 		disease Nutritional and Metabolic Diseases Disease or Syndrome 21 4 0.010 None 1.000 1 2018 2018
CUI: C0342883
Disease: Cholesteryl Ester Transfer Protein Deficiency
Cholesteryl Ester Transfer Protein Deficiency 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 22 5 0.400 None 0.923 38 1 1989 2018
CUI: C4290140
Disease: recurrent myocardial infarction
recurrent myocardial infarction 		disease Disease or Syndrome 22 6 0.010 None < 0.001 1 1 2013 2013
CUI: C0020476
Disease: Hyperlipoproteinemias
Hyperlipoproteinemias 		disease Nutritional and Metabolic Diseases Disease or Syndrome 23 7 0.310 None 1.000 1 1990 2001
CUI: C0948242
Disease: Nuchal bleb, familial
Nuchal bleb, familial 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Immune System Diseases; Hemic and Lymphatic Diseases Congenital Abnormality 23 9 0.010 None 1.000 1 2014 2014
CUI: C1963961
Disease: Testosterone deficiency
Testosterone deficiency 		disease Disease or Syndrome 24 1 0.010 None 1.000 1 2006 2006
CUI: C3160761
Disease: Diabetic dyslipidaemia
Diabetic dyslipidaemia 		disease Disease or Syndrome 28 11 0.030 None 1.000 3 1 2014 2017
CUI: C0020479
Disease: Hyperlipoproteinemia Type III
Hyperlipoproteinemia Type III 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 28 20 0.020 None 1.000 2 1994 1994